Canonical Allele Identifier: CA346672647

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170895A>C (hg19) ; chr2:g.43943756A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943756A>C , CM000664.2:g.43943756A>C	GRCh38
NC_000002.11:g.44170895A>C , CM000664.1:g.44170895A>C	GRCh37
NC_000002.10:g.44024399A>C	NCBI36
NG_008247.1:g.57250T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.2435T>G	ENSP00000386562.2:p.Ile812Ser
ENST00000447246.2:c.2435T>G	ENSP00000403637.2:p.Ile812Ser
ENST00000681961.1:n.2455T>G
ENST00000682104.1:c.2309T>G	ENSP00000507716.1:p.Ile770Ser
ENST00000682303.1:c.*2221T>G	ENSP00000508325.1:n.*2221T>G
ENST00000682308.1:c.2435T>G	ENSP00000507056.1:p.Ile812Ser
ENST00000682480.1:c.2435T>G	ENSP00000508344.1:p.Ile812Ser
ENST00000682546.1:c.2432T>G	ENSP00000508188.1:p.Ile811Ser
ENST00000682585.1:c.2435T>G	ENSP00000506885.1:p.Ile812Ser
ENST00000682595.1:n.3017T>G
ENST00000682607.1:c.853T>G
ENST00000682779.1:c.2426T>G	ENSP00000507947.1:p.Ile809Ser
ENST00000682845.1:n.1537T>G
ENST00000682885.1:c.2390T>G	ENSP00000508036.1:p.Ile797Ser
ENST00000682933.1:n.2509T>G
ENST00000683072.1:n.3017T>G
ENST00000683125.1:c.2435T>G	ENSP00000507939.1:p.Ile812Ser
ENST00000683213.1:c.2438T>G	ENSP00000507751.1:p.Ile813Ser
ENST00000683220.1:c.2465T>G	ENSP00000507151.1:p.Ile822Ser
ENST00000683329.1:n.3238T>G
ENST00000683346.1:c.*2310T>G	ENSP00000507458.1:n.*2310T>G
ENST00000683459.1:n.3022T>G
ENST00000683590.1:c.2435T>G	ENSP00000506820.1:p.Ile812Ser
ENST00000683623.1:c.2342T>G	ENSP00000507702.1:p.Ile781Ser
ENST00000683645.1:n.2986T>G
ENST00000683694.1:n.1186T>G
ENST00000683796.1:c.*2307T>G	ENSP00000508221.1:n.*2307T>G
ENST00000683802.1:n.5360T>G
ENST00000683833.1:c.2426T>G	ENSP00000506852.1:p.Ile809Ser
ENST00000683989.1:c.2435T>G	ENSP00000507510.1:p.Ile812Ser
ENST00000683994.1:c.2435T>G	ENSP00000507181.1:p.Ile812Ser
ENST00000684290.1:c.*129T>G	ENSP00000507243.1:n.*129T>G
ENST00000684306.1:c.*2348T>G	ENSP00000508384.1:n.*2348T>G
ENST00000684341.1:n.2455T>G
ENST00000684383.1:c.*2073T>G	ENSP00000506863.1:n.*2073T>G
ENST00000684397.1:c.139T>G
ENST00000684619.1:c.*2307T>G	ENSP00000508088.1:n.*2307T>G
ENST00000684743.1:n.3466T>G
ENST00000260665.12:c.2435T>G MANE Select	ENSP00000260665.7:p.Ile812Ser
ENST00000260665.11:c.2435T>G	ENSP00000260665.7:p.Ile812Ser
NM_133259.3:c.2435T>G	NP_573566.2:p.Ile812Ser
XM_006711915.2:c.2357T>G	XP_006711978.1:p.Ile786Ser
XM_006711916.2:c.2435T>G	XP_006711979.1:p.Ile812Ser
XM_011532473.1:c.2435T>G	XP_011530775.1:p.Ile812Ser
XM_011532474.1:c.2435T>G	XP_011530776.1:p.Ile812Ser
XM_006711916.3:c.2435T>G	XP_006711979.1:p.Ile812Ser
XM_017003117.1:c.2357T>G	XP_016858606.1:p.Ile786Ser
XR_002958896.1:n.2477T>G
NM_133259.4:c.2435T>G MANE Select	NP_573566.2:p.Ile812Ser